Special Education Versus Inclusive Education: The Role of the TEACCH Program
2009-01-01 Panerai, S; Zingale, M; Trubia, G; Finocchiaro, M; Zuccarello, R; Ferri, R; Elia, M
EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME
1994-01-01 Musumeci, Sa; Elia, M; Ferri, R; Scuderi, C; Delgracco, S
Trisomy 12p and epilepsy with myoclonic absences
1998-01-01 Elia, M; Musumeci, Sa; Ferri, R; Cammarata, M
Epilepsy in the Setting of Full Trisomy 18: A Multicenter Study on 18 Affected Children With and Without Structural Brain Abnormalities
2016-01-01 Matricardi, Sara; Spalice, Alberto; Salpietro, Vincenzo; Di Rosa, Gabriella; Balistreri Maria, Cristina; Grosso, Salvatore; Parisi, Pasquale; Elia, M; Striano, Pasquale; Accorsi, Patrizia; Cusmai, Raffaella; Specchio, Nicola; Coppola, Giangennaro; Savasta, Salvatore; Carotenuto, Marco; Tozzi, Elisabetta; Ferrara, Pietro; Ruggieri, Martino; Verrotti, Alberto
Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics
2015-01-01 Wilmshurst Jo, M.; Gaillard William, D.; Vinayan Kollencheri, Puthenveettil; Tsuchida Tammy, N.; Plouin, Perrine; Van Bogaert, Patrick; Carrizosa, Jaime; Elia, M; Craiu, Dana; Jovic Nebojsa, J.; Nordli, Doug; Hirtz, Deborah; Wong, Virginia; Glauser, Tracy; Mizrahi Eli, M.; Cross J., Helen
Clinical Significance of Rare Copy Number Variations in Epilepsy A Case-Control Survey Using Microarray-Based Comparative Genomic Hybridization
2012-01-01 Striano, P; Coppola, A; Paravidino, R; Malacarne, M; Gimelli, S; Robbiano, A; Traverso, M; Pezzella, M; Belcastro, V; Bianchi, A; Elia, M; Falace, A; Gazzerro, E; Ferlazzo, E; Freri, E; Galasso, R; Gobbi, G; Molinatto, C; Cavani, S; Zuffardi, O; Striano, S; Ferrero, Gb; Silengo, M; Cavaliere, Ml; Benelli, M; Magi, A; Piccione, M; Bricarelli, Fd; Coviello, Da; Fichera, M; Minetti, C; Zara, F
Color mapping of middle-latency somatosensory evoked potentials in autistic mentally retarded children
1997-01-01 Ferri, R; Elia, M; Delgracco, S; Musumeci, Sa; Stefanini, Mc
CLINICAL AND NEUROPHYSIOLOGICAL ASPECTS OF EPILEPSY IN SUBJECTS WITH AUTISM AND MENTAL-RETARDATION
1995-01-01 Elia, M; Musumeci, Sa; Ferri, R; Bergonzi, P
Sleep neurophysiology in fragile X patients
1995-01-01 Musumeci, Sa; Ferri, R; Elia, M; Dalgracco, S; Scuderi, C; Stefanini, Mc; Castano, A; Azan, G
Peculiar dyschromic changes of finger nails in a patient with multiple system atrophy
1998-01-01 Siragusa, M; Del Gracco, S; Elia, M; Ferri, R; Schepis, C
EMOTIONAL FACIAL PARALYSIS IN THE RETT SYNDROME
1991-01-01 Pereira, Jlp; Elia, M; Ferri, R
Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes
2007-01-01 Bonati, Mt; Russo, S; Finelli, P; Valsecchi, Mr; Cogliati, F; Cavalleri, F; Roberts, W; Elia, M; Larizza, L
Sleep phenotypes of intellectual disability: A polysomnographic evaluation in subjects with Down syndrome and Fragile-X syndrome
2008-01-01 Miano, S; Bruni, O; Elia, M; Scifo, L; Smerieri, A; Trovato, A; Verrillo, E; Terzano, Mg; Ferri, R
Nonlinear EEG analysis during sleep in premature and full-term newborns
2003-01-01 Ferri, R; Chiaramonti, R; Elia, M; Musumeci, Sa; Ragazzoni, A; Stam, Cj
Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins
2008-01-01 Diani, E; Di Bonaventura, C; Mecarelli, O; Gambardella, A; Elia, M; Bovo, G; Bisulli, F; Pinardi, F; Binelli, S; Egeo, G; Castellotti, B; Striano, P; Striano, S; Bianchi, A; Ferlazzo, E; Vianello, V; Coppola, G; Aguglia, U; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C
Mild generalized epilepsy and developmental disorder associated with large inv dup(15)
2002-01-01 Chifari, R; Guerrini, R; Pierluigi, M; Cavani, S; Sgro, V; Elia, M; Canger, R; Canevini, Mp
Age- and height-dependent changes of amplitude and latency of somatosensory evoked potentials in children and young adults with Down's syndrome
1996-01-01 Ferri, R; Delgracco, S; Elia, M; Musumeci, Sa; Stefanini, Mc
Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNA(Cys) gene
2007-01-01 Scuderi, C; Borgione, E; Musumeci, S; Elia, M; Castello, F; Fichera, M; Davidzon, G; Dimauro, S
Chromosome abnormalities and epilepsy
2001-01-01 Elia, M; Musumeci, Sa; Ferri, R; Ayala, Gf
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression
2009-01-01 Lintas, C; Sacco, R; Garbett, K; Mirnics, K; Militerni, R; Bravaccio, C; Curatolo, P; Manzi, B; Schneider, C; Melmed, R; Elia, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Special Education Versus Inclusive Education: The Role of the TEACCH Program | 1-gen-2009 | Panerai, S; Zingale, M; Trubia, G; Finocchiaro, M; Zuccarello, R; Ferri, R; Elia, M | |
| EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 1-gen-1994 | Musumeci, Sa; Elia, M; Ferri, R; Scuderi, C; Delgracco, S | |
| Trisomy 12p and epilepsy with myoclonic absences | 1-gen-1998 | Elia, M; Musumeci, Sa; Ferri, R; Cammarata, M | |
| Epilepsy in the Setting of Full Trisomy 18: A Multicenter Study on 18 Affected Children With and Without Structural Brain Abnormalities | 1-gen-2016 | Matricardi, Sara; Spalice, Alberto; Salpietro, Vincenzo; Di Rosa, Gabriella; Balistreri Maria, Cristina; Grosso, Salvatore; Parisi, Pasquale; Elia, M; Striano, Pasquale; Accorsi, Patrizia; Cusmai, Raffaella; Specchio, Nicola; Coppola, Giangennaro; Savasta, Salvatore; Carotenuto, Marco; Tozzi, Elisabetta; Ferrara, Pietro; Ruggieri, Martino; Verrotti, Alberto | |
| Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics | 1-gen-2015 | Wilmshurst Jo, M.; Gaillard William, D.; Vinayan Kollencheri, Puthenveettil; Tsuchida Tammy, N.; Plouin, Perrine; Van Bogaert, Patrick; Carrizosa, Jaime; Elia, M; Craiu, Dana; Jovic Nebojsa, J.; Nordli, Doug; Hirtz, Deborah; Wong, Virginia; Glauser, Tracy; Mizrahi Eli, M.; Cross J., Helen | |
| Clinical Significance of Rare Copy Number Variations in Epilepsy A Case-Control Survey Using Microarray-Based Comparative Genomic Hybridization | 1-gen-2012 | Striano, P; Coppola, A; Paravidino, R; Malacarne, M; Gimelli, S; Robbiano, A; Traverso, M; Pezzella, M; Belcastro, V; Bianchi, A; Elia, M; Falace, A; Gazzerro, E; Ferlazzo, E; Freri, E; Galasso, R; Gobbi, G; Molinatto, C; Cavani, S; Zuffardi, O; Striano, S; Ferrero, Gb; Silengo, M; Cavaliere, Ml; Benelli, M; Magi, A; Piccione, M; Bricarelli, Fd; Coviello, Da; Fichera, M; Minetti, C; Zara, F | |
| Color mapping of middle-latency somatosensory evoked potentials in autistic mentally retarded children | 1-gen-1997 | Ferri, R; Elia, M; Delgracco, S; Musumeci, Sa; Stefanini, Mc | |
| CLINICAL AND NEUROPHYSIOLOGICAL ASPECTS OF EPILEPSY IN SUBJECTS WITH AUTISM AND MENTAL-RETARDATION | 1-gen-1995 | Elia, M; Musumeci, Sa; Ferri, R; Bergonzi, P | |
| Sleep neurophysiology in fragile X patients | 1-gen-1995 | Musumeci, Sa; Ferri, R; Elia, M; Dalgracco, S; Scuderi, C; Stefanini, Mc; Castano, A; Azan, G | |
| Peculiar dyschromic changes of finger nails in a patient with multiple system atrophy | 1-gen-1998 | Siragusa, M; Del Gracco, S; Elia, M; Ferri, R; Schepis, C | |
| EMOTIONAL FACIAL PARALYSIS IN THE RETT SYNDROME | 1-gen-1991 | Pereira, Jlp; Elia, M; Ferri, R | |
| Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes | 1-gen-2007 | Bonati, Mt; Russo, S; Finelli, P; Valsecchi, Mr; Cogliati, F; Cavalleri, F; Roberts, W; Elia, M; Larizza, L | |
| Sleep phenotypes of intellectual disability: A polysomnographic evaluation in subjects with Down syndrome and Fragile-X syndrome | 1-gen-2008 | Miano, S; Bruni, O; Elia, M; Scifo, L; Smerieri, A; Trovato, A; Verrillo, E; Terzano, Mg; Ferri, R | |
| Nonlinear EEG analysis during sleep in premature and full-term newborns | 1-gen-2003 | Ferri, R; Chiaramonti, R; Elia, M; Musumeci, Sa; Ragazzoni, A; Stam, Cj | |
| Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins | 1-gen-2008 | Diani, E; Di Bonaventura, C; Mecarelli, O; Gambardella, A; Elia, M; Bovo, G; Bisulli, F; Pinardi, F; Binelli, S; Egeo, G; Castellotti, B; Striano, P; Striano, S; Bianchi, A; Ferlazzo, E; Vianello, V; Coppola, G; Aguglia, U; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C | |
| Mild generalized epilepsy and developmental disorder associated with large inv dup(15) | 1-gen-2002 | Chifari, R; Guerrini, R; Pierluigi, M; Cavani, S; Sgro, V; Elia, M; Canger, R; Canevini, Mp | |
| Age- and height-dependent changes of amplitude and latency of somatosensory evoked potentials in children and young adults with Down's syndrome | 1-gen-1996 | Ferri, R; Delgracco, S; Elia, M; Musumeci, Sa; Stefanini, Mc | |
| Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNA(Cys) gene | 1-gen-2007 | Scuderi, C; Borgione, E; Musumeci, S; Elia, M; Castello, F; Fichera, M; Davidzon, G; Dimauro, S | |
| Chromosome abnormalities and epilepsy | 1-gen-2001 | Elia, M; Musumeci, Sa; Ferri, R; Ayala, Gf | |
| Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression | 1-gen-2009 | Lintas, C; Sacco, R; Garbett, K; Mirnics, K; Militerni, R; Bravaccio, C; Curatolo, P; Manzi, B; Schneider, C; Melmed, R; Elia, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, Kl; Persico, Am |
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